FDA recall Z-0361-2019

Inpeco S.A. · Class II · device

Product

FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) (same product) FlexLab, Accelerator a3600 and Aptio Automation are modular systems designed to automate Pre- Analytical and Post-Analytical processing,

Reason for recall

The firm has identified customer sites where there are modules on which the safety pacemaker label is missing. The information regarding the label included in the Operations Manual has been updated to specify that: 1) the risk of a pacemaker malfunction applies to anyone with a pacemaker who may work on these modules; and 2) the minimum safety distance has been increased to 200 mm (7.87") from the transport mechanisms. Any person with a pacemaker must not get closer than this distance from the modules axes.

Distribution

Foreign distribution to Netherlands, Italy, Belgium, Austria, France, Spain, and Germany.

Key facts

Status
Terminated
Initiation date
2018-08-24
Report date
2018-11-07
Termination date
2020-03-19
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lugano, N/A, Switzerland

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0361-2019